allergy relief-d (11822-9994)

Drug Facts

Product Profile

Brand Name allergy relief-d

Generic Name cetirizine hydrochloride and pseudoephedrine hydrochloride

Labeler rite aid

Dosage Form TABLET, FILM COATED, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

cetirizine hydrochloride 5 mg/1, pseudoephedrine hydrochloride 120 mg/1

Manufacturer

RITE AID

Identifiers & Regulatory

Product NDC 11822-9994

Product ID 11822-9994_2ac6ca2f-a821-90d4-e063-6394a90a023f

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA090922

Listing Expiration 2026-12-31

Marketing Start 2023-07-20

Pharmacologic Class

Classes

adrenergic alpha-agonists [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 118229994

Hyphenated Format 11822-9994

Supplemental Identifiers

RxCUI

1014571

UNII

64O047KTOA 6V9V2RYJ8N

Packaging Origin

Original Packager

true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name allergy relief-d (source: ndc)

Generic Name cetirizine hydrochloride and pseudoephedrine hydrochloride (source: ndc)

Application Number ANDA090922 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

5 mg/1
120 mg/1

source: ndc

Packaging

2 BLISTER PACK in 1 CARTON (11822-9994-1) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (11822-9994-2)

source: ndc

Packages (2)

11822-9994-1 2 BLISTER PACK in 1 CARTON (11822-9994-1) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK 11822-9994-2 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (11822-9994-2)

Ingredients (2)

cetirizine hydrochloride (5 mg/1) pseudoephedrine hydrochloride (120 mg/1)

Linked Drug Pages (1)

Allergy relief-D ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "2ac6ca2f-a821-90d4-e063-6394a90a023f", "openfda": {"unii": ["64O047KTOA", "6V9V2RYJ8N"], "rxcui": ["1014571"], "spl_set_id": ["1bf7c028-1648-4211-8847-84cce833a0f1"], "manufacturer_name": ["RITE AID"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (11822-9994-1)  / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "11822-9994-1", "marketing_start_date": "20230720"}, {"sample": false, "description": "6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (11822-9994-2)", "package_ndc": "11822-9994-2", "marketing_start_date": "20230720"}], "brand_name": "Allergy relief-D", "product_id": "11822-9994_2ac6ca2f-a821-90d4-e063-6394a90a023f", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "11822-9994", "generic_name": "Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride", "labeler_name": "RITE AID", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy relief-D", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA090922", "marketing_category": "ANDA", "marketing_start_date": "20230720", "listing_expiration_date": "20261231"}